Cas 73870-16-3,Methyl-2-acetoxymethyl-5-benzyloxycarbonyl-4-methoxycarbonylethylpyrrol-3-propionat

73870-16-3

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Basic information

Product Name: Methyl-2-acetoxymethyl-5-benzyloxycarbonyl-4-methoxycarbonylethylpyrrol-3-propionat
Synonyms: Methyl-2-acetoxymethyl-5-benzyloxycarbonyl-4-methoxycarbonylethylpyrrol-3-propionat
CAS NO:73870-16-3
Molecular Formula:
Molecular Weight: 445.469
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Methyl-2-acetoxymethyl-5-benzyloxycarbonyl-4-methoxycarbonylethylpyrrol-3-propionat(CAS DataBase Reference)
NIST Chemistry Reference: Methyl-2-acetoxymethyl-5-benzyloxycarbonyl-4-methoxycarbonylethylpyrrol-3-propionat(73870-16-3)
EPA Substance Registry System: Methyl-2-acetoxymethyl-5-benzyloxycarbonyl-4-methoxycarbonylethylpyrrol-3-propionat(73870-16-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 73870-16-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73870-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,7 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73870-16:
(7*7)+(6*3)+(5*8)+(4*7)+(3*0)+(2*1)+(1*6)=143
143 % 10 = 3
So 73870-16-3 is a valid CAS Registry Number.

73870-16-3Upstream product

73870-16-3Downstream Products

73870-16-3Relevant academic research and scientific papers

Tetrapyrrole Biosynthesis, 10. - Easy Biomimetic Porphyrin Syntheses

Franck, Burchhard,Bringmann, Gerhard,Wegner, Christian,Spiegel, Udo

, p. 263 - 274 (2007/10/02)

The hitherto unknown porphyrin octacarboxylic acids 12a and 20a can be prepared in a highly selective reaction by acid catalysed condensation of monopyrroles, which are structurally related to porphobilinogen (1), the precursor of porphyrin biosynthesis.T

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